Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Oct 2001

Cormier T A, Prakash S K, Magner D B, Zoghbi H Y, Van den Veyver I B

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blotting, Northern
Share to GTPase-Activating Proteins
Share to Ligases
Share to Lyases

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mice, Mutant Strains

Share to Microtubule Proteins

Share to Polydactyly

Share to X Chromosome

Source

Identifiers

PMID: 11668396
DOI: 10.1007/s00335-001-1006-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice.PMID 11668396Read ↗

High-throughput discovery of novel developmental phenotypes.Semantic proximity Read ↗

Contributions to the MODY5 phenotype.Semantic proximity Read ↗

Jagged1 (JAG1): Structure, expression, and disease associations.Semantic proximity Read ↗

Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the PhenotypeSemantic proximity Read ↗

Using human sequencing to guide craniofacial researchSemantic proximity Read ↗

The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.Semantic proximity Read ↗

The MID1 gene product in physiology and disease.Semantic proximity Read ↗

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.Semantic proximity Read ↗

Untangling the pathways of SDHx loss of function.Semantic proximity Read ↗

Cardiac malformations and midline skeletal defects in mice lacking filamin A.Semantic proximity Read ↗

Disruption of the Fbxw8 gene results in pre- and postnatal growth retardation in mice.Semantic proximity Read ↗

The first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.